FDA Adverse Event Malfunction Summary report: N

BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES

MDR report key: 1000755 · Received February 19, 2008

Report

Report Number
1219602-2008-00024
Event Type
Malfunction
Date Received
February 19, 2008
Report Date
November 7, 2008
Manufacturer
SMITH & NEPHEW INC., ENDOSCOPY DIV.
Product Code
MBI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BIORAPTOR 2.9 SUTURE ANCHOR W/ TWO SUTURES BIORAPTOR MBI SMITH & NEPHEW INC., ENDOSCOPY DIV. 7210706 50230834

Patients

Seq Age Sex Outcome Treatment
1 NA